Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thiophene | HCID 8030 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 53854495 | HCID 53854495 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53754573 | HCID 53754573 | 39% |
Reaction Steps
A mixture of N-(4-nitro-2,6-dichlorophenyl)-4-formyl-1-piperazineacetamide (1.79 g crude) was suspended in methanol (50 mL) containing 4% methanolic thiophene (0.5 mL) and 5% platinum on charcoal catalyst (900 mg). This was hydrogenated using a Parr apparatus for 30 minutes at 50° C. and 26 psi. After filtration and the removal of solvent in vacuo, the filtrate yielded 1.38 g of crude residue. This was subjected to flash chromatography on deactivated silica gel (from a slurry of 300 g of silica gel in methylene chloride containing 3.4 mL of conc. NH4OH). The product was eluted with CH2Cl2 :MeOH:NH4OH 98.8:1.0:0.2 yielding 590 mg of III an off-white solid. This was triturated in methylene chloride-ether to yield a white solid (520 mg, 39% yield).: m.p.>220° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05382584 |
|---|
| Source dataset | uspto-grants-1995_01 |
|---|
| ORD ID | ord-f8c900d661c44be09050d2c2b1cac2b7 |
|---|
| Source note | uspto-grants-1995_01 |
|---|